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FDA 510(k)

FUORECAM

K-Number: K093705 · 2010-04-23

ApplicantTherapeutic Technologies, Inc.
Decision Date2010-04-23
Product CodeNBL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FUORECAM is the device name listed in this FDA 510(k) record. The listed applicant is Therapeutic Technologies, Inc.. It received FDA 510(k) clearance on 2010-04-23 under 510(k) number K093705. The device is classified under product code NBL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUORECAM?

FUORECAM is a medical device that received FDA 510(k) clearance on 2010-04-23. The listed applicant is Therapeutic Technologies, Inc.. The 510(k) number is K093705.

When did FUORECAM receive FDA 510(k) clearance?

FUORECAM received FDA 510(k) clearance on 2010-04-23, under 510(k) number K093705.

Who is the listed applicant for FUORECAM?

The FDA 510(k) record lists Therapeutic Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FUORECAM?

The FDA product code for FUORECAM is NBL.

Related Clinical Trials

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Other records listing Therapeutic Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K900029SPECTRASTIM 2000 MUSCLE STIMULATORK893964SPECTRASTIM TM 1000K854277NEUROPATH 4000K841112TTI REHABILATATION GYM SYS

Related Devices (Code: NBL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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